Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_assertion description "[Several apoE and LPL gene variants affecting CAD risk, plasma TG or apoB concentrations have an allelic frequency of >5% in the general population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_assertion evidence source_evidence_literature NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_assertion SIO_000772 17848837 NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_assertion wasDerivedFrom gad-20150221 NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_assertion wasGeneratedBy ECO_0000203 NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP111671.RAtAW65X-eRQXvP2kx6GbpQyUX2SjRynXIVjzb92XNMOc130_provenance.